首页> 美国卫生研究院文献>Frontiers in Oncology >CXCL13/CXCR5 Axis Predicts Poor Prognosis and Promotes Progression Through PI3K/AKT/mTOR Pathway in Clear Cell Renal Cell Carcinoma
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CXCL13/CXCR5 Axis Predicts Poor Prognosis and Promotes Progression Through PI3K/AKT/mTOR Pathway in Clear Cell Renal Cell Carcinoma

机译:CXCL13 / CXCR5轴通过透明细胞肾细胞癌的PI3K / AKT / mTOR途径预测不良预后并促进进展

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摘要

The chemokine ligands and their receptors play critical roles in cancer progression and patients outcomes. We found that CXCL13 was significantly upregulated in ccRCC tissues compared with normal tissues in both The Cancer Genome Atlas (TCGA) cohort and a validated cohort of 90 pairs ccRCC tissues. Statistical analysis showed that high CXCL13 expression related to advanced disease stage and poor prognosis in ccRCC. We also revealed that serum CXCL13 levels in ccRCC patients (n = 50) were significantly higher than in healthy controls (n = 40). Receiver operating characteristic (ROC) curve revealed that tissue and serum CXCL13 expression might be a diagnostic biomarker for ccRCC with an area under curve (AUC) of 0.809 and 0.704, respectively. CXCL13 was significantly associated with its receptor, CXCR5, in ccRCC tissues, and ccRCC patients in high CXCL13 high CXCR5 expression group have a worst prognosis. Functional and mechanistic study revealed that CXCL13 promoted the proliferation and migration of ccRCC cells by binding to CXCR5 and activated PI3K/AKT/mTOR signaling pathway. These results suggested that CXCL13/CXCR5 axis played a significant role in ccRCC and might be a therapeutic target and prognostic biomarker.
机译:趋化因子配体及其受体在癌症进展和患者预后中起关键作用。我们发现,在癌症基因组图谱(TCGA)队列和经过验证的90对ccRCC组织中,与正常组织相比,ccRCC组织中的CXCL13明显上调。统计分析表明,高表达CXCL13与ccRCC的疾病晚期和不良预后有关。我们还发现ccRCC患者(n = 50)的血清CXCL13水平显着高于健康对照(n = 40)。受体工作特征(ROC)曲线显示组织和血清CXCL13表达可能是ccRCC的诊断生物标志物,曲线下面积(AUC)分别为0.809和0.704。 CXCL13在ccRCC组织中与其受体CXCR5显着相关,在高CXCL13高CXCR5表达组的ccRCC患者的预后最差。功能和机理研究表明,CXCL13通过与CXCR5结合并激活PI3K / AKT / mTOR信号通路来促进ccRCC细胞的增殖和迁移。这些结果表明,CXCL13 / CXCR5轴在ccRCC中起着重要作用,可能是治疗靶点和预后的生物标志物。

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